Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/04—Ortho-condensed systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/02—Non-specific cardiovascular stimulants, e.g. drugs for syncope, antihypotensives

Definitions

• the present invention relates to the compounds of formula: ##STR2## their salts, their preparation, the intermediates for preparing them and medicinal products containing them.
• R and R 1 which are identical or different, represent a hydrogen or halogen atom or an alkyl, alkoxy, amino, acylamino, phenylureido, --N ⁇ CH--N(R 2 )R 3 , nitro, imidazolyl phenyl, SO 3 H or cyano radical
• R 2 and R 3 which are identical or different, each represent an alkyl radical.
• the alkyl and alkoxy radicals contain 1 to 4 carbon atoms in a linear or branched chain and the acyl radicals and portions contain 2 to 5 carbon atoms.
• the halogen atoms are preferably bromine, chlorine and fluorine atoms.
• the compounds of formula (I) may be prepared by dealkylation and desalification of the derivatives of formula: ##STR3## in which R and R 1 have the same meanings as in formula (I), R 4 represents an alkyl radical and Hal represents a halogen atom and, preferably, a bromine atom.
• This reaction is preferably carried out in the presence of imidazole, at a temperature of between 100° and 200° C. and in particular at 160° C.
• the derivatives of formula (II) may be obtained by the action of a derivative of formula: ##STR4## in which R 4 has the same meanings as in formula (II), on a 2-haloindanone of formula: ##STR5## in which R and R 1 have the same meanings as in formula (I) and Hal represents a halogen atom and, preferably, a bromine atom.
• This reaction is generally carried out in an inert solvent such as dimethylformamide, at a temperature of between 50° and 150° C. and, preferably, at 115° C.
• an inert solvent such as dimethylformamide
• the derivatives of formula (III) may be obtained by adapting or applying the method described by D. D. DAVEY, J. Org. Chem., 52, 4379 (1987).
• the derivatives of formula (IV) may be obtained by halogenation of the corresponding indanones by means of a halogenating agent such as bromine or chlorine, in an inert solvent such as a chlorine-containing solvent (for example methylene chloride or chloroform), at a temperature of -15° C. or in acetic acid, at a temperature close to 20° C., or a copper halide, in dioxane, at a temperature close to 100° C. or by applying or adapting the methods described by K. MORI, Agr. Biol. Chem., 27 (1), 22 (1963); J. CHAKRAVARTY, Indian J. Chem., 7 (3), 215 (1969), F. G.
• a halogenating agent such as bromine or chlorine
• an inert solvent such as a chlorine-containing solvent (for example methylene chloride or chloroform)
• a chlorine-containing solvent for example methylene chloride or chloroform
• the indanones may be obtained by applying or adapting the methods described by M. OLIVIER et al., Bull. Soc. Chim. de France, 3092 (1973), R. SEKA et al., Chem. Ber., 75B, 1730 (1942), in U.S. Pat. Nos. 4,263,319, 4,096,173 and EP 314400 and in the examples.
• the compounds of formula (I) may also be prepared by cyclization of a derivative of formula: ##STR6## in which R and R 1 have the same meanings as in formula (I).
• This cyclization is carried out by means of an acid such as acetic acid or hydrochloric acid, in aqueous medium or in an alcohol such as ethanol or methanol, optionally in the presence of ammonium acetate, at the boiling temperature of the reaction medium.
• an acid such as acetic acid or hydrochloric acid
• aqueous medium or in an alcohol such as ethanol or methanol
• an alcohol such as ethanol or methanol
• the derivatives of formula (V) may be obtained by the action of ammonia on a derivative of formula: ##STR7## in which R and R 1 have the same meanings as in formula (I) and alk represents an alkyl radical.
• This reaction is carried out in an alcohol such as methanol or ethanol, at a temperature of between 20° C. and the boiling temperature of the reaction medium.
• an alcohol such as methanol or ethanol
• the derivatives of formula (VI) may be obtained by the action of a 2-haloindanone of formula (IV) on a derivative of formula: ##STR8## in which alk has the same meanings as in formula (VI).
• This reaction is carried out either by fusion at a temperature of between 130° and 180° C., or in an inert solvent such as dimethylformamide in the presence of a base such as an alkali metal hydride (for example sodium hydride), at a temperature close to 20° C., or in an inert solvent such as a chlorine-containing solvent such as chloroform in the presence of a nitrogen-containing organic base (for example 1,8-diazabicyclo 5.4.0!undec-7-ene), at a temperature close to 20° C., or in an inert solvent such as an alcohol (for example ethanol or propanol), an aromatic solvent such as toluene, a chlorine-containing solvent (for example chloroform), optionally in the presence of sodium iodide, at the boiling temperature of the reaction medium.
• a base such as an alkali metal hydride (for example sodium hydride)
• an inert solvent such as a chlorine-containing solvent such as chloroform in the presence of a
• the derivatives of formula (VII) may be obtained by applying or adapting the method described in U.S. Pat. No. 3,600,399.
• the compounds of formula (I) for which R and/or R 1 represent a nitro radical may also be prepared by nitration of a corresponding compound of formula (I) for which R and/or R 1 represent a hydrogen atom.
• This nitration is generally carried out by means of a nitrating agent such as an alkali metal nitrate (preferably potassium nitrate), in sulphuric acid at a temperature of 0° C. to 30° C.
• a nitrating agent such as an alkali metal nitrate (preferably potassium nitrate), in sulphuric acid at a temperature of 0° C. to 30° C.
• the compounds of formula (I) for which R and/or R 1 represent an amino radical may also be prepared by reducing a corresponding compound of formula (I) for which R and/or R 1 represent a nitro radical.
• This reduction is generally carried out by means of hydrogen, at a pressure of 1 to 2 bar, in the presence of aqueous sodium hydroxide and a catalyst such as palladium on carbon, at a temperature close to 20° C.
• the compounds of formula (I) for which R and/or R 1 represent an SO 3 H radical may also be prepared by sulphonating a corresponding derivative of formula (I) for which R and/or R 1 represent a hydrogen atom.
• This reaction is generally carried out by means of chlorosulphonic acid, at a temperature of between 0° and 20° C.
• the compounds of formula (I) for which R and/or R 1 represent an acylamino radical may also be prepared by acylating a corresponding compound of formula (I) for which R and/or R 1 represent an amino radical.
• This acylation is generally carried out in an inert solvent such as dimethylformamide, by means of an acid anhydride (alk-CO) 2 O in which alk represents an alkyl radical containing 1 to 4 carbon atoms, in the presence of a base such as a trialkylamine (for example triethylamine), at the boiling temperature of the reaction medium.
• alk-CO acid anhydride
• the compounds of formula (I) for which R and/or R 1 represent a phenylureido radical may also be prepared by the action of phenyl isocyanate on a corresponding compound of formula (I) for which R and/or R 1 represent an amino radical.
• This reaction is generally carried out in an inert solvent such as dimethyl sulphoxide, dimethylformamide, a chlorine-containing solvent (for example chloroform), in the presence of a base such as a trialkylamine (for example triethylamine), at a temperature close to 20° C.
• an inert solvent such as dimethyl sulphoxide, dimethylformamide, a chlorine-containing solvent (for example chloroform)
• a base such as a trialkylamine (for example triethylamine)
• the compounds of formula (I) for which R and/or R 1 represent a radical --N ⁇ CH--N(R 2 )R 3 may also be prepared by the action of a corresponding compound of formula (I) for which R and/or R 1 represent an amino radical on an amide HCO--N(R 2 )R 3 in which R 2 and R 3 have the same meanings as in formula (I).
• This reaction is preferably carried out in the presence of methylsulphonyl chloride and a base such as a trialkylamine (for example triethylamine), at a temperature close to 20° C.
• a base such as a trialkylamine (for example triethylamine)
• the compounds of formula (I) may be purified by the usual known methods, for example by crystallization, chromatography or extraction.
• the E and Z isomers of the compounds of formula (I) for which R and/or R 1 represent a radical --N ⁇ CH--N(R 2 )R 3 may be separated by the usual known methods, for example by crystallization or chromatography.
• the compounds of formula (I) containing a basic residue may be optionally converted to addition salts with an inorganic or organic acid by the action of such an acid in an organic solvent such as an alcohol, a ketone, an ether or a chlorine-containing solvent.
• organic solvent such as an alcohol, a ketone, an ether or a chlorine-containing solvent.
• the compounds of formula (I) containing an acidic residue may be optionally converted to metallic salts or to addition salts with nitrogen-containing bases according to methods known per se. These salts may be obtained by the action of a metallic (for example alkali metal or alkaline-earth metal) base, ammonia, an amine or a salt of an amine on a compound of formula (I), in a solvent. The salt formed is separated by the usual methods.
• a metallic for example alkali metal or alkaline-earth metal
• salts with inorganic or organic acids such as acetate, propionate, succinate, benzoate, fumarate, maleate, oxalate, methanesulphonate, isethionate, theophyllinacetate, salicylate, methylene-bis- ⁇ -oxynaphthoate, hydrochloride, sulphate, nitrate and phosphate
• the salts with alkali metals sodium, potassium and lithium
• alkaline-earth metals calcium and magnesium
• the salt of ammonium the salts of nitrogen-containing bases (ethanolamine, trimethylamine, methylamine, benzylamine, N-benzyl- ⁇ -phenethylamine, choline, arginine, leucine, lysine, N-methylglucamine).
• the compounds of formula (I) have useful pharmacological properties. These compounds are antagonists of the ⁇ -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor, also known as quisqualate receptor.
• AMPA ⁇ -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
• the compounds of formula (I) are non-competitive antagonists of the N-methyl-D-aspartate (NMDA) receptor and, more particularly, they are ligands for the glycine modulating sites of the NMDA receptor.
• NMDA N-methyl-D-aspartate
• These compounds are therefore useful for treating or preventing all ischemias (such as focal or global ischemia) following cerebral vascular accidents, a cardiac arrest, an arterial hypotension, a cardiac or pulmonary surgical operation or a severe hypoglycemia. They are generally useful in the treatment of effects due to an anoxia, whether perinatal or following a drowning or cerebrospinal lesions. These compounds may also be used for treating or preventing the progression of neurodegenerative diseases, of HUNTINGTON'S chorea, of ALZHEIMER'S disease, of amyotrophic lateral sclerosis, of olivopontocerebellar atrophy and of PARKINSON'S disease.
• These compounds may also be used against epileptogenic and/or convulsive manifestations, for the treatment of cerebral and spinal traumas, for the treatment of anxiety (KEHNE et al., Eur. J. Pharmacol., 193, 283 (1991), depression (TRULLAS et al., Eur. J. Pharmacol., 185, 1 (1990), schizophrenia (REYNOLDS, TIPS, 13, 116 (1992), as analgesics (DICKENSON et al., Neurosc.
• the affinity of the compounds of formula (I) for the AMPA receptor was determined by studying the antagonism of the specific binding of 3 H!-AMPA to rat cerebral cortex membranes (HONORE et al., Neuroscience letters, 54, 27 (1985)).
• 3 H!-AMPA is incubated in the presence of 0.2 mg of proteins at 4° C. for 30 minutes in 10 mM KH 2 PO 4 , 100 mM KSCN buffer, pH 7.5.
• Non-specific binding is determined in the presence of 1 mM L-glutamate.
• the bound radioactivity is separated by filtration on PHARMACIA filters (Printed Filtermate A).
• the inhibitory activity of these products is generally less than 100 ⁇ m.
• the affinity of the compounds of formula (I) for the glycine site linked to the NMDA receptor was determined by studying the antagonism of the specific binding of 3 H!-DCKA to rat cerebral cortex membranes according to the method described by T. CANTON et al., J. Pharm. Pharmacol., 44, 812 (1992).
• 3 H!-DCKA (20 nM) is incubated in the presence of 0.1 mg of proteins at 4° C. for 30 minutes in 50 mM HEPES buffer, pH 7.5.
• Non-specific binding is determined in the presence of 1 mM glycine.
• the bound radioactivity is separated by filtration on Whatman GF/B filters.
• the inhibitory activity of these products is generally less than 100 ⁇ M.
• the compounds of formula (I) have a low toxicity. Their LD 50 is greater than 50 mg/kg by the IP route in mice.
• R represents a hydrogen atom and R 1 is in position 7, 8 or 9 and represents a hydrogen or halogen atom or an alkyl, alkoxy, amino, acylmmino, phenylureido, --N ⁇ CH--N(R 2 )R 3 , nitro, imidazolyl, phenyl or SO 3 H radical; or R represents a halogen atom and R 1 represents a halogen atom or a nitro radical.
• the 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared in the following manner: 2.2 g of ethyl 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate are dissolved in 80 ml of a 2.5N ammoniacal methanol solution and the solution is kept for 20 hours at a temperature close to 20° C. and then concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 35° C.
• the product obtained is suspended in 50 ml of isopropyl ether, filtered, washed twice with a total of 20 ml of isopropyl ether and then dried under reduced pressure (15 mmHg; 2 kPa) at a temperature close to 20° C. 1.85 g of 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide are thus obtained in the form of a solid which melts at 221° C.
• the ethyl 1-(5-fluoro-1-oxo-2-indanyl)-imidazole-2-carboxylate can be prepared in the following manner: a solution of 13.3 g of ethyl imidazole-2-carboxylate in 145 ml of anhydrous dimethylformamide is added dropwise over 20 minutes at a temperature of between 20° C. and 25° C. to a suspension of 3.4 g of 80% sodium hydride in 45 ml of anhydrous dimethylformamide maintained under a nitrogen atmosphere.
• the product obtained (27 g) is chromatographed on 1490 g of neutral silica gel (0.020-0.045 mm) contained in a column 9.6 cm in diameter, eluting under pressure with a dichloromethane-ethyl acetate mixture (70-30 by volume) and collecting 80 ml fractions. Fractions 13 to 70 are pooled and concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C. 13.4 g of ethyl 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate are thus obtained which melt at 127° C.
• the 2-bromo-5-fluoro-1-indanone can be prepared in the following manner: a solution of 20.6 g of bromine in 90 ml of acetic acid is added dropwise over 1 hour at 20° C. to a solution of 20 g of 5-fluoro-1-indanone and 0.1 ml of a 47% aqueous hydrobromic acid solution in 260 ml of acetic acid. After stirring for 2 hours, the mixture is poured over 850 ml of distilled water and extracted 3 times with a total of 850 ml of methylene chloride.
• the organic extracts are pooled, washed with 200 ml of distilled water, dried over anhydrous sodium sulphate and concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 30° C.
• the product obtained (31 g) is chromatographed on 1860 g of neutral silica gel (0.020-0.045 mm) contained in a column 9.8 cm in diameter, eluting with a cyclohexane-ethyl acetate mixture (70-30 by volume) and collecting a fraction of 10.5 litres which is removed and then a fraction of 25 liters which is concentrated under reduced pressure (15 mmHg; 2 kPa) at 40° C.
• Example 2 The procedure is carried out as in Example 1 but starting with 1.8 g of 1-(5-methyl-1-oxo-2-indanyl)imidazole-2-carboxamide, a total of 80 ml of methanol and 22 ml of 12N aqueous hydrochloric acid solution. 1.5 g of 8-methyl-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one hydrochloride are thus obtained which decompose without melting above 300° C.
• the 1-(5-methyl-1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared as in Example 1 for the preparation of 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide but starting with 2.4 g of ethyl 1-(5-methyl-1-oxo-2-indanyl)imidazole-2-carboxylate and 75 ml of a 2.5N ammoniacal methanol solution. 1.9 g of 1-(5-methyl-1-oxo-2-indanyl)imidazole-2-carboxamide are thus obtained in the form of a solid which melts at 196° C.
• the ethyl 1-(5-methyl-1-oxo-2-indanyl)imidazole-2-carboxylate can be prepared as in Example 1 for the preparation of ethyl 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate but starting with 2.24 g of ethyl imidazole-2-carboxylate, 0.6 g of 80% sodium hydride, 4.6 g of 2-bromo-5-methyl-1-indanone and a total of 62 ml of anhydrous dimethylformamide.
• the 2-bromo-5-methyl-1-indanone can be prepared as in Example 1 for the preparation of 2-bromo-5-fluoro-1-indanone but starting with 7.3 g of 5-methyl-1-indanone, 8 g of bromine, 0.05 ml of a 47% aqueous hydrobromic acid solution and a total of 165 ml of acetic acid. After silica gel chromatography with a cyclohexane-dichloromethane mixture (70-30 by volume), 4.6 g of 2-bromo-5-methyl-1-indanone are obtained which melt at 54° C.
• Example 2 The procedure is carried out as in Example 1 but starting with 2 g of 1-(4-methyl-1-oxo-2-indanyl)imidazole-2-carboxamide, a total of 60 ml of methanol and 25 ml of 12N aqueous hydrochloric acid solution. 1.45 g of 9-methyl-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one hydrochloride are thus obtained which decompose without melting above 300° C.
• the 1-(4-methyl-1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared as in Example 1 for the preparation of 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide but starting with 2.7 g of ethyl 1(4-methyl-1-oxo-2-indanyl)imidazole-2-carboxylate and 160 ml of a 2.5N ammoniacal methanol solution. 2.1 g of 1-(4-methyl-1-oxo-2-indanyl)imidazole-2-carboxamide are thus obtained in the form of a solid which melts at 160° C.
• the ethyl-1-(4-methyl-1-oxo-2-indanyl)-imidazole-2-carboxylate can be prepared as in Example 1 for the preparation of ethyl 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate but starting with 2.8 g of ethyl imidazole-2-carboxylate, 0.7 g of 80% sodium hydride, 4.6 g of 2-bromo-4-methyl-1-indanone and a total of 75 ml of anhydrous dimethylformamide.
• the 2-bromo-4-methyl-1-indanone can be prepared as described by K. MORI, Agr. Biol. Chem., 27 (1), 22 (1963).
• Example 2 The procedure is carried out as in Example 1 but starting with 1 g of 1-(6-chloro-1-oxo-2-indanyl)imidazole-2-carboxamide, a total of 75 ml of methanol and 15 ml of 12N aqueous hydrochloric acid solution. 0.4 g of 7-chloro-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one hydrochloride is obtained which decomposes without melting above 300° C.
• the 1-(6-chloro-1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared as in Example 1 for the preparation of 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide but starting with 1.2 g of ethyl 1-(6-chloro-1-oxo-2-indanyl)imidazole-2-carboxylate and 45 ml of a 2.5N ammoniacal methanol solution. 1 g of 1-(6-chloro-1-oxo-2-indanyl)imidazole-2-carboxamide is thus obtained in the form of a solid which melts at 190° C.
• the ethyl 1-(6-chloro-1-oxo-1-indanyl)imidazole-2-carboxylate can be prepared as in Example 1 for the preparation of ethyl 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate but starting with 2.5 g of ethyl imidazole-2-carboxylate, 0.7 g of 80% sodium hydride, 5.4 g of 2-bromo-6-chloro-1-indanone and a total of 70 ml of anhydrous dimethylformamide.
• the 2-bromo-6-chloro-1-indanone can be prepared as described in German Patent 2,640,358.
• Example 2 The procedure is carried out as in Example 1 but starting with 0.84 g of 1-(5-chloro-1-oxo-2-indanyl)imidazole-2-carboxamide, a total of 55 ml of methanol and 4 ml of a 12N aqueous hydrochloric acid solution. 0.64 g of 8-chloro-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one hydrochloride is thus obtained which decomposes without melting above 300° C.
• the 1-(5-chloro-1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared in the following manner: a solution of 1.2 g of ethyl 1-(5-chloro-1-oxo-2-indanyl)imidazole-2-carboxylate in 45 ml of methanol is maintained saturated for 6 hours, with boiling, with a stream of azunonia gas. After cooling to 5° C., the crystals are separated by filtration, washed with 1 ml of ice-cold methanol and air dried at 20° C. 0.4 g of 1-(5-chloro-1-oxo-2-indanyl)imidazole-2-carboxamide is thus obtained in the form of a solid which melts at 240° C.
• the ethyl 1-(5-chloro-1-oxo-2-indanyl)imidazole-2-carboxylate can be prepared in the following manner: a solution of 3.65 g of 1,8-diazabicyclo 5.4.0!undec-7-ene in 10 ml of chloroform is added dropwise over 20 minutes at a temperature close to 20° C. to a solution of 2.8 g of ethyl imidazole-2-carboxylate and 6.1 g of 2-bromo-5-chloro-1-indanone.
• the 2-bromo-5-chloro-1-indanone can be prepared as described in German Patent 2,640,358.
• Example 2 The procedure is carried out as in Example 1 but starting with 1.4 g of 1-(4-chloro-1-oxo-2-indanyl)imidazole-2-carboxamide, a total of 70 ml of methanol and 21 ml of a 12N aqueous hydrochloric acid solution. 0.53 g of 9-chloro-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one is thus obtained which decomposes without melting above 300° C.
• the 1-(4-chloro-1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared in the following manner: a solution of 1.8 g of ethyl 1-(4-chloro-1-oxo-2-indanyl)imidazole-2-carboxylate in 170 ml of a 2.5N ammoniacal methanol solution is kept for 16 hours at a temperature close to 20° C. and then concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 50° C.
• the product obtained is suspended in 30 ml of isopropyl ether, filtered, washed twice with a total of 10 ml of isopropyl ether and then dried under reduced pressure (15 mmHg; 2 kPa) at a temperature close to 20° C.
• 1.4 g of 1-(4-chloro-1-oxo-2-indanyl)imidazole-2-carboxamide are thus obtained in the form of a solid which melts at 90° C.
• the ethyl 1-(4-chloro-1-oxo-2-indanyl)-imidazole-2-carboxylate can be prepared as in Example 1 for the preparation of ethyl 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate but starting with 2.8 g of ethyl imidazole-2-carboxylate, 0.6 g of 80% sodium hydride, 6.4 g of 2-bromo-4-chloro-1-indanone and a total of 80 ml of anhydrous dimethylformamide.
• the 2-bromo-4-chloro-1-indanone can be prepared in the following manner: a solution of 16 g of bromine in 45 ml of acetic acid is added dropwise over 30 minutes at a temperature close to 20° C. to a suspension of 17.5 g of 4-chloro-1-indanone in a mixture of 240 ml of acetic acid and 0.1 ml of a 47% aqueous hydrobromic acid solution. After stirring for 2 hours at the same temperature, the mixture is poured over 380 ml of distilled water. The crystals are separated hy filtration, washed twice with a total of 60 ml of distilled water and dried under reduced pressure (15 mmHg; 2 kPa) at 45° C.
• the 4-chloro-1-indanone can be prepared as described in U.S. Pat. No. 4,096,173.
• Example 2 The procedure is carried out as in Example 1 but starting with 0.5 g of 1-(4-phenyl-1-oxo-2-indanyl)imidazole-2-carboxamide, a total of 60 ml of methanol and 8 ml of a 12N aqueous hydrochloric acid solution. 0.35 g of 9-phenyl1-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one hydrochloride is thus obtained which decomposes without melting above 300° C.
• the 1-(4-phenyl-1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared as in Example 1 for the preparation of 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide but starting with 0.64 g of ethyl 1-(5-methyl-1-oxo-2-indanyl)imidazole-2-carboxylate and 80 ml of a 5N ammoniacal methanol solution. 0.5 g of 1-(4-phenyl-1-oxo-2-indanyl)imidazole-2-carboxamide is thus obtained in the form of a solid which melts at 196° C.
• the ethyl 1-(4-phenyl-1-oxo-2-indanyl)imidazole-2-carboxylate can be prepared in the following manner: a mixture of 1.1 g of ethyl imidazole-2-carboxylate and 1.15 g of 2-bromo-4-phenyl-1-indanone is heated for 20 minutes at 130° C., cooled to 20° C. and dissolved in 25 ml of dichloromethane. The solution is washed with 10 ml of distilled water and, after decanting, the aqueous phase is extracted twice with a total of 20 ml of dichloromethane.
• the organic phases are pooled, washed with 10 ml of a saturated sodium hydrogen carbonate solution, twice with a total of 20 ml of distilled water, dried over anhydrous sodium sulphate and concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 35° C.
• the product obtained (1.55 g) is chromatographed on 155 g of neutral silica gel (0.020-0.045mm) contained in a column 3.3 cm in diameter, eluting under pressure with a dichloromethane-ethyl acetate mixture (80-20 by volume) and collecting 10-ml fractions.
• the 2-bromo-4-phenyl-1-indanone can be prepared as in Example 1 for the preparation of 2-bromo-5-fluoro-1-indanone but starting with 2.65 g of 4-phenyl-1-indanone, 2 g of bromine, 0.1 ml of a 47% aqueous hydrobromic acid solution and a total of 55 ml of acetic acid. After silica gel chromatography with a cyclohexane-dichloromethane mixture (50-50 by volume), 2.1 g of 2-bromo-4-phenyl-1-indanone are obtained which melt at 98° C.
• the 4-phenyl-1-indanone can be prepared as described in U.S. Pat. No. 4,263,319.
• Example 2 The procedure is carried out as in Example 1 but starting with 0.46 g of 1- 5-(1-imidazolyl)-1-oxo-2-indanyl!imidazole-2-carboxamide, a total of 35 ml of methanol and 7 ml of a 12N aqueous hydrochloric acid solution. 0.23 of 8-(1-imidazolyl)-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazine-4-one hydrochloride is thus obtained which decomposes without melting above 300° C.
• the 1- 5-(1-imidazolyl)-1-oxo-2-indanyl!-imidazole-2-carboxamide can be prepared as in Example 1 for the preparation of 1-(5-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide but starting with 0.6 g of ethyl 1- 5-(1-imidazolyl)-1-oxo-2-indanyl!imidazole-2-carboxylate and 30 ml of a 2.5N ammoniacal methanol solution. 0.46 g of 1- 5-(1-imidazolyl)-1-oxo-2-indanyl!imidazole-2-carboxamide is thus obtained in the form of a solid which melts at 140° C.
• the ethyl 1- 5-(1-imidazolyl)-1-oxo-2-indanyl!imidazole-2-carboxylate can be prepared in the following manner: 1.1 g of bromine is added at 70° C. to a solution of 1.2 g of 5-(1-imidazolyl)-1-indanone in a mixture of 10 ml of acetic acid and 0.5 ml of a 47% aqueous hydrobromic acid solution. After stirring for 30 minutes at the same temperature, the mixture is poured over 50 ml of distilled water, neutralized by adding 15 g of sodium carbonate and extracted 4 times with a total of 90 ml of dichloromethane.
• the organic extracts are pooled, washed with 20 ml of a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulphate, supplemented with 10 ml of anhydrous dimethylformamide and the dichloromethane is selectively removed under reduced pressure (15 mmHg; 2 kPa) at 40° C.
• the solution in dimethylformamide thus obtained (10 ml) is added dropwise over 5 minutes at 25° C. to a solution of 0.7 g of ethyl imidazole-2-carboxylate in 10 ml of anhydrous dimethylformamide previously supplemented as in Example 1 with 0.7 g of 80% sodium hydride.
• the 5-(1-imidazolyl)-1-indanone can be prepared as described in European Patent 314 400.
• the product obtained (0.5 g) is dissolved in 50 ml of a 2N aqueous sodium hydroxide solution and then the mixture is acidified to pH 2 by addition of a 1N aqueous hydrochloric acid solution.
• the insoluble matter which appears is separated by filtration, successively washed 3 times with a total of 30 ml of distilled water, 3 times with a total of 30 ml of acetone and with 10 ml of ethyl ether and then dried under reduced pressure (1 mmHg; 0.13 kPa) at 50° C.
• the product (1.7 g) is chromatographed on 100 g of neutral silica gel (0.020-0.045 mm) contained in a column 3.2 cm in diameter, eluting under pressure with a dichloromethane-methanol mixture (97-7 by volume) and collecting 10-ml fractions.
• the fractions 35 to 182 are pooled and concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C.
• the product obtained (0.6 g) is dissolved in a boiling mixture of 64 ml of dimethylformamide and 16 ml of distilled water and the solution, supplemented with decolorizing charcoal, is filtered hot, cooled and kept for 16 hours at 5° C.
• the 3,7-dimethyl-4-oxo-5H, 10H-imidazo 1,2-a!-indeno 1,2-e!pyrazinium bromide can be prepared in the following manner: a solution of 4.75 g of 2-bromo-6-methyl-1-indanone and 2 g of 1-methyl-1H-imidazole-2-carboxamide in 40 ml of anhydrous dimethylformamide is stirred for 16 hours at 115° C. and cooled to 20° C. The crystals are separated by filtration, washed twice with a total of 20 ml of ethyl ether and dried under reduced pressure (15 mmHg; 2 kPa) at 50° C.
• the 2-bromo-6-methyl-1-indanone can be prepared as described by J. CHAKRAVARTY, Indian J. Chem., 7(3), 215 (1969).
• the product thus obtained (4 g) is dissolved in 80 ml of dimethylformamide and the solution, supplemented with 20 g of silica, is concentrated to dryness under reduced pressure (15 mmHg, 2 kPa) at 100° C.
• the mixture is introduced into a column 4.2 cm in diameter containing 240 g of silica and it is then eluted with a dichloromethane-methanol mixture (97-3 by volume), collecting 60-ml fractions.
• Fractions 10 to 70 are pooled, supplemented with 1.5 g of decolorizing charcoal, filtered and concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 55° C.
• the product obtained (1.7 g) is dissolved in 350 ml of boiling methanol and the solution, supplemented with 0.1 g of decolorizing charcoal, is filtered hot, concentrated under reduced pressure (15 mmHg; 2 kPa) at 40° C. in order to adjust its volume to about 30 ml and then preserved at 5° C. for 60 hours.
• the crystals are separated by filtration, washed twice with a total of 20 ml of ice-cold methanol and dried under reduced pressure (1 mmHg; 0.13 kPa) at 60° C.
• 1.1 g of 5H, 10H-imidazo 1,2-a!-- indeno 1,2-e!pyrazin-4-one are thus obtained which decompose without melting at 350° C.
• Rf 0.77, thin-layer chromatography on silica gel, solvent: dichloromethane-methanol (8-2 by volume)!.
• the 3-methyl-4-oxo-5H, 10H-imidazo 1,2-a!-indeno 1,2-e!pyrazinium bromide can be prepared in the following manner: a solution of 5 g of 1-methyl-1H-imidazole-2-carboxamide and 12 g of 85% 2-bromoindanone in 100 ml of anhydrous dimethylformamide is stirred for 28 hours at 115° C. and then cooled to a temperature close to 20° C. The insoluble matter is separated by filtration, washed twice with a total of 20 ml of ice-cold dimethylformamide and dried under reduced pressure (10 mmHg; 1.3 kPa).
• the 1-methyl-1H-imidazole-2-carboxamide can be prepared according to the process described by D. D. DAVEY, J. Org. Chem., 52, 4379 (1987).
• Example 2 The procedure is carried out as in Example 1 starting with 3.8 g of 1-(5-bromo-1-oxo-2-indanyl)imidazole-2-carboxamide, a total of 420 ml of methanol and 57 ml of a 12N aqueous hydrochloric acid solution. 3 g of 8-bromo-5H, 10H-imidazo 1,2-a!indeno- 2-e!pyrazin-4-one hydrochloride are thus obtained which decompose without melting above 300° C.
• the 1-(5-bromo-1-oxo-2-- indanyl)imidazole-2-carboxamide can be prepared as in Example 1 for the preparation of 1-(5-fluoro-1-oxo-2-- indanyl)imidazole-2-carboxamide but starting with 3.7 g of ethyl 1-(5-bromo-1-oxo-2-- indanyl)imidazol e -2-carboxylate and 300 ml of a 5N ammoniacal methanol solution. 3.2 g of 1-(5-bromo-1-oxo-2-- indanyl)imidazole-2-carboxamide are thus obtained in the form of a solid which melts at 240° C.
• the ethyl 1-(5-bromo-1-oxo-2-indanyl)imidazole-2-carboxylate can be prepared in the following manner: a solution of 9.5 g of ethyl imidazole-2-carboxylate, 9.9 g of 2,5-dibromo-1-indanone and 0.1 g of sodium iodide in 280 ml of ethanol is kept boiling for 16 hours, cooled to 20° C. and dried under reduced pressure (20 mmHg; 2.6 kPa) at 50° C.
• the product obtained (21 g) is dissolved in 50 ml of dichloromethane and the solution is washed 3 times with a total of 600 ml of distilled water, dried over anhydrous magnesium sulphate and dried under reduced pressure (20 mmHg; 2.6 kPa) at 50° C.
• the product obtained (12.7 g) is chromatographed on 790 g of neutral silica gel (0.020-0.045 mm) contained in a column 7 cm in diameter, eluting under pressure with a dichloromethane-ethyl acetate mixture (70-30 by volume) and collecting 75-ml fractions.
• the 2,5-dibromo-1-indanone can be prepared as described in European Patent 346107.
• the 1-(4-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide can be obtained in the following manner: 720 mg of ethyl 1-(4-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate are dissolved in 50 ml of a 3N ammoniacal methanol solution and the solution is kept stirring for 20 hours at a temperature close to 20° C., and then concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C. The residue thus obtained is purified by flash chromatography on a silica column, under a nitrogen stream at medium pressure (0.5 bar) with ethyl acetate as eluent. 420 mg of 1-(4-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide are thus obtained which melt at 159° C.
• the ethyl 1-(4-fluoro-1-oxo-2-indanyl)-imidazole-2-carboxylate can be obtained in the following manner: the solution of 5.3 g of ethyl imidazole-2-carboxylate in 20 ml of anhydrous dimethylformamide is added dropwise over 30 minutes at a temperature close to 20° C. to a suspension of 2.43 g of 50% sodium hydride in 60 ml of anhydrous dimethylformamide kept under a nitrogen atmosphere. After stirring for 15 minutes, a solution of 9.26 g of 2-bromo-4-fluoro-1-indanone in 25 ml of anhydrous dimethylformamide is added dropwise over 30 minutes at a temperature close to 20° C.
• the 2-bromo-4-fluoro-1-indanone can be obtained in the following manner: to a solution of 8 g of 4-fluoro-1-indanone in 400 ml of dioxane, are added 31.3 g of copper bromide. The solution is then heated to a temperature close to 100° C. for 4 hours. The reaction medium is then filtered on celite and then concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C. 13.23 g of 2-bromo-4-fluoro-1-indanone is thus obtained which is used as it is in subsequent syntheses.
• the 4-fluoro-1-indanone can be prepared as described by M. OLIVIER and E. MARECHAL, Bull. Soc. Chim. Fr., (11), 3042 (1973).
• Example 14 The procedure is carried out as in Example 14 but starting with 0.26 g of 1-(6,7-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide, 80 ml of methanol and 20 ml of hydrochloric acid (12N). 97 mg of 6,7-dichloro-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one are thus obtained in hydrochloride form which melt at a temperature greater than 260° C. (analysis: % calculated C: 49.35, H: 2.44, Cl: 29.88, N: 13.28, % found C: 49.40, H: 2.10, Cl: 29.90, N: 13.10).
• the 1-(6,7-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared as in Example 14 for the preparation of 1-(4-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide but starting with 1 g of ethyl 1-(6,7-dichloro-1-oxo-2-indanyl)imidazole-2-carboxylate and 56 ml of a 3N ammoniacal methanol solution. 270 mg of 1-(6,7-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide are thus obtained which melt at 270° C.
• the ethyl 1-(6,7-dichloro-1-oxo-2-indanyl)-imidazole-2-carboxylate can be prepared as in Example 14 for the preparation of ethyl 1-(4-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate but starting with 2.5 g of ethyl imidazole-2-carboxylate, 0.65 g of 80% sodium hydride, 6.06 g of 2-bromo-6,7-dichloro-1-indanone and a total of 36 ml of anhydrous dimethylformamide.
• the 2-bromo-6,7-dichloro-1-indanone is prepared as in Example 14 for the preparation of 2-bromo-4-fluoro-1-indanone but starting with 7.42 g of 6,7-dichloro-1-indanone, 21.8 g of copper bromide and 240 ml of dioxane. After purification by silica column chromatography with an ethyl acetate-cyclohexane mixture (10-90 by volume) as eluent, 6.79 g of 2-bromo-6,7-dichloro-1-indanone are obtained which melt at 103° C.
• the 6,7-dichloro-1-indanone can be prepared in the following manner: 58.8 g of 3-(3,4-dichlorophenyl)propionic acid and 315 ml of thionyl chloride are refluxed for 45 minutes. After removing, by distillation, the excess thionyl chloride, 1200 ml of anhydrous dichloromethane and 47 g of aluminium chloride are added. The reaction medium is refluxed for 6 hours, cooled and 1366 ml of a 1N aqueous hydrochloric acid solution are added.
• the 3-(3,4-dichlorophenyl)propionic acid can be prepared in the following manner: to a solution of 69.86 g of 3,4-dichlorocinnamic acid, 1750 ml of methanol and 21 g of hexahydrated nickel chloride, there are added over 75 minutes, while the temperature is kept close to 20° C., 57.75 g of sodium borohydride. After stirring for one hour at a temperature close to 20° C., the solution is filtered and then concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C.
• the residue thus obtained is dissolved in 875 ml of an aqueous potassium hydroxide solution (5%) and extracted with 1000 ml of ethyl ether.
• the aqueous phase is acidified with 945 ml of a 2N aqueous hydrochloric acid solution and then extracted with two times 1000 ml of ethyl ether.
• the organic phase is dried over anhydrous magnesium sulphate, concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C. and 58.8 g of 3-(3,4-dichlorophenyl)propionic acid are obtained which melt at 90° C.
• Example 14 The procedure is carried out as in Example 14 but starting with 0.11 g of 1-(7,8-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide, 10 ml of methanol and 35 ml of hydrochloric acid (12N). 30 mg of 7,8-dichloro-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one are thus obtained in hydrochloride form which melt at a temperature greater than 260° C.
• infrared spectrum (KBr)characteristic bands in cm -1 : 3425, 3200 to 2125, 2000, 3125, 3140, 3020, 1710 and shoulder at 1695, 1645, 1550, 1500, 1450, 1385, 1105, 780 and 675!.
• the 1-(7,8-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide is prepared as in Example 14 for the preparation of 1-(4-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide but starting with 0.18 g of ethyl 1-(7,8-dichloro-1-oxo-2-indanyl)imidazole-2-carboxylate and 10 ml of a 3N ammoniacal methanol solution. 0.13 mg of 1-(7,8-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide is thus obtained which melts at 264° C.
• the ethyl 1-(7,8-dichloro-1-oxo-2-indanyl)imidazole-2-carboxylate is prepared as in Example 14 for the preparation of ethyl 1-(4-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate but starting with 1.66 g of ethyl imidazole-2-carboxylate, 0.47 g of 80% sodium hydride, 4 g of 2-bromo-5,6-dichloro-1-indanone and a total of 24 ml of anhydrous dimethylformamide.
• the 2-bromo-5,6-dichloro-1-indanone is prepared as in Example 14 for the preparation of 2-bromo-4-fluoro-1-indanone but starting with 5.48 g of 5,6-dichloro-1-indanone, 16.1 g of copper bromide and 175 ml of dioxane. After purifying by silica column chromatography with an ethyl acetate-cyclohexane mixture (10-90 by volume) as eluent, 4.07 g of 2-bromo-5,6-dichloro-1-indanone are obtained which melt at 85° C.
• Example 14 The procedure is carried out as in Example 14 but starting with 0.72 g of 1-(8,9-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide, 220 ml of methanol and 55 ml of hydrochloric acid (12N). 0.57 g of 8,9-dichloro-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one is thus obtained in hydrochloride form which melts at a temperature greater than 260° C. (analysis: % calculated C: 53.45, H: 2.42, Cl: 24.27, N: 14.38, O: 5.4, % found C: 53.50, H: 2.50, Cl: 23.50, N: 14.40, O: 5.8).
• the 1-(8,9-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared as in Example 14 for the preparation of 1-(4-fluoro-1-oxo-2-indanyl)imidazole-2-carboxamide but starting with 1.77 g of ethyl 1-(8,9-dichloro-1-oxo-2-indanyl)imidazole-2-carboxylate and 95 ml of a 3N ammoniacal methanol solution. 0.66 g of 1-(8,9-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide is thus obtained which melts at 202° C.
• the ethyl 1-(8,9-dichloro-1-oxo-2-indanyl)imidazole-2-carboxylate can be prepared in the following manner: a mixture of 4.2 g of ethyl imidazole-2-carboxylate and 4.2 g of 2-bromo-4,5-dichloro-1-indanone is heated at 130° C. for 20 minutes, cooled to 20° C. and dissolved in 90 ml of dichloromethane. The solution is washed with 35 ml of water.
• the 2-bromo-4,5-dichloro-1-indanone can be prepared as in Example 14 for the preparation of 2-bromo-4-fluoro-1-indanone but starting with 12.67 g of 4,5-dichloro-1-indanone, 37.3 g of copper bromide and 400 ml of dioxane. 16.79 g of 2-bromo-6,7-dichloro-1-indanone are thus obtained which melt at 131° C.
• the 4,5-dichloro-1-indanone is prepared as in Example 15 for the preparation of 6,7-dichloro-1-indanone but star6ing with 26 g of 3-(2,3-dichlorophenyl)propionic acid, 138 ml of thionyl chloride, 550 ml of anhydrous dichloromethane and 20.5 g of aluminium chloride. After recrystallization from 100 ml of boiling ethanol, 12.67 g of 4,5-dichloro-1-indanone are thus obtained which melt at 78° C.
• the 3-(2,3-dichlorophenyl)propionic acid can be prepared as in Example 15 for the preparation of 3-(3,4-dichlorophenyl)propionic acid but starting with 33 g of 2,3-dichlorocinnamic acid, 800 ml of methanol and 9.9 g of hexahydrated nickel chloride and 27.22 g of sodium borohydride. 26.33 g of 3-(2,3-dichlorophenyl)propionic acid are obtained which melt at 100° C.
• Example 14 The procedure is carried out as in Example 14 but starting with 1.27 g of 1-(7,9-dichloro-1-oxo-2-indanyl)imidazole-2-carboxamide, 390 ml of methanol and 96 ml of hydrochloric acid (12N). 1.44 g of 7,9-dichloro-5H, 10H-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one are thus obtained in hydrochloride form which melt at a temperature greater than 260° C. (analysis: % calculated C: 47.52, H: 2.45, Cl: 32.37, N: 12.79, O: 4.87, % found C: 47.20, H: 2.30, Cl: 32.10, N: 12.70, O: 4.80).
• the ethyl 1-(7,9-dichloro-1-oxo-2-indanyl)-imidazole-2-carboxylate can be prepared in the following manner: a mixture of 7.25 g of ethyl imidazole-2-carboxylate and 7.25 g of 2-bromo-4,6-dichloro-1-indanone is heated at 130° C. for 30 minutes, cooled to 20° C. and dissolved in 100 ml of dichloromethane. The solution is washed with 200 ml of water.
• the organic phase is washed with 200 ml of a saturated aqueous sodium bicarbonate solution, 240 ml of distilled water, dried over anhydrous sodium sulphate and concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C.
• the residue thus obtained is purified by flash chromatography on a silica column with an ethyl acetate-cyclohexane mixture (80-20 by volume) as eluent. 2.90 g of ethyl 1-(7,9-dichloro-1-oxo-2-indanyl)imidazole-2-carboxylate are thus obtained which melt at 127° C.
• the 2-bromo-4,6-dichloro-1-indanone is prepared as in Example 14 for the preparation of 2-bromo-4-fluoro-1-indanone but starting with 21.6 g of 4,6-dichloro-1-indanone, 63.56 g of copper bromide and 690 ml of dioxane. 14.5 g of 2-bromo-4,6-dichloro-1-indanone are obtained which melt at 80° C.
• the 4,6-dichloro-1-indanone can be prepared as in Example 15 for the preparation of 6,7-dichloro-1-indanone but starting with 53 g of 3-(2,4-dichlorophenyl)propionic acid, 284 ml of thionyl chloride, 1130 ml of anhydride dichloromethane and 42.16 g of aluminium chloride. After recrystallization from 150 ml of boiling ethanol, 21.62 g of 4,6-dichloro-1-indanone are obtained which melt at 120° C.
• the 3-(2,4-dichlorophenyl)propionic acid can be prepared as in Example 15 for the preparation of 3-(3,4-dichlorophenyl)propionic acid but starting with 66 g of 2,4-dichlorocinnamic acid, 1600 ml of methanol, 19.8 g of hexahydrated nickel chloride and 54.44 g of sodium borohydride. 53.44 g of 3-(2,4-dichlorophenyl)-propionic acid are thus obtained which melt at 83° C.
• the 9-bromo-5H, 10H-imidazo 1,2-a!indeno- 1,2-e!pyrazin-4-one can be prepared in the following manner: 4.6 g of 1-(4-bromo-1-oxo-2-indanyl)imidazole-2-carboxamide are dissolved in 350 ml of boiling methanol and the solution, supplemented with 0.2 g of decolorizing charcoal, is filtered hot, concentrated under reduced pressure (15 mmHg; 2 kPa) at 40° C. To the residue thus obtained, there are added 150 ml of 12N hydrochloric acid and the solution is preserved at 5° C. for 18 hours. The crystals are separated by filtration and redissolved in 150 ml of boiling methanol.
• the 1-(4-bromo-1-oxo-2-indanyl)imidazole-2-carboxamide can be obtained in the following manner: a solution of 3.5 g of ethyl 1-(4-bromo-1-oxo-2-indanyl)imidazole-2-carboxylate in 20 ml of methanol is maintained saturated for one hour, with boiling, with a stream of ammonia gas. The reaction medium is then concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C. 3.10 g of 1-(4-bromo-1-oxo-2-indanyl)imidazole-2-carboxamide are thus obtained which melt at 212° C.
• the ethyl 1-(4-bromo-1-oxo-2-indanyl)-imidazole-2-carboxylate can be obtained in the following manner: a mixture of 9.28 g of ethyl imidazole-2-carboxylate and 8.50 g of 2,4-dibromo-1-indanone is heated at 130° C. for 20 minutes, cooled to 20° C. and dissolved in 50 ml of dichloromethane. The solution is washed twice with 100 ml of water.
• the organic phase is washed with 50 ml of a 0.1N aqueous sodium hydroxide solution, 300 ml of distilled water, dried over anhydrous sodium sulphate and concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C.
• the residue thus obtained is purified by flash chromatography on a silica column, under a nitrogen stream at medium pressure (0.5 bar) with ethyl acetate as eluent.
• 3.5 g of ethyl 1-(4-bromo-1-oxo-2-indanyl)-imidazole-2-carboxylate are thus obtained which melt at 157° C.
• the 2,4-dibromo-1-indanone can be obtained in the following manner: a solution of 24 g of 4-bromo-1-indanone and 120 ml of chloroform is cooled to 5° C. A solution of 18.2 g of bromine and 20 ml of chloroform is then added dropwise over two hours at a temperature of between 0° and 5° C. stirring leaving the reaction medium stirring for one hour while maintaining the introduction temperature, the solution is allowed to return to room temperature and it is further stirred for one hour. The reaction medium is then concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 40° C.
• the 4-bromo-1-indanone can be prepared as described by F. G. HOLLIMAN, F. G. MANNE and D. A. THORNTON, J. Chem. Soc., 9 (1960).
• the ethyl 1-(5-methoxy-1-oxo-2-indanyl)-imidazole-2-carboxylate can be prepared in the following manner: a mixture of 13.9 g of 2-bromo-5-methoxy-1-indanone and 16.2 g of 2-ethoxycarbonyl-imidazole in 300 ml of toluene is refluxed for 9 hours. The toluene is then evaporated under reduced pressure and the residue is taken up in dichloromethane and water. The organic phase is extracted with dichloromethane and washed with water.
• the crude product is purified by two successive silica column chromatographies with mixtures of dichloromethane and ethyl acetate (70/30 by volume) and dichloromethane and methanol (98/2 by volume) respectively.
• the 2-bromo-5-methoxy-1-indanone can be synthesized as described by D. MUXHOPADHYA, D. N. CHAUDHURY, J. Indian Chem. Soc., 47(5), 450 (1970).
• a mixture of 9.7 g of 5H, 10H-8-nitro-imidazo 1,2-a!indeno 1,2-e!pyrazin-4-one, 370 ml of 0.1N aqueous sodium hydroxide and 0.3 g of 10% palladized carbon is hydrogenated at a temperature close to 20° C. under a pressure of 1.2 bar for 23 hours.
• the suspension is acidified with 80 ml of 1N hydrochloric acid, then it is filtered.
• the solid obtained is taken up in 600 ml of boiling water.
• the mixture is supplemented with animal charcoal and filtered hot on celite.
• the filtrate crystallizes after cooling on an ice bath. The crystals are separated by filtration and washed twice with 50 ml of ethyl ether.
• the ethyl 1-(6-fluoro-1-oxo-2-indanyl)imidazole-2-carboxylate can be prepared in the following manner: 12.8 g of ethyl imidazole-2-carboxylate and 10.1 g of 2-bromo-6-fluoroindanone are heated at 130° C. for 20 minutes. After cooling to a temperature close to 20° C., the mixture is taken up in 100 ml of dichloromethane, washed twice with 30 ml of 0.1N sodium hydroxide and then 3 times with 40 ml of distilled water.
• the 2-bromo-6-fluoroindanone can be prepared in the following manner: a solution of 6.4 g of bromine in 30 ml of acetic acid is added dropwise over 25 min at 20° C. to a solution of 12 g of 6-fluoroindanone and 0.05 ml of a 47% aqueous hydrobromic acid solution in 100 ml of acetic acid. After stirring for 5 hours, the mixture is poured over crushed ice. The precipitate formed is filtered, washed with distilled water and then with petroleum ether. 10.1 g of the expected product are thus obtained in the form of a beige solid which melts at 98° C.
• the 6-fluoroindanone can be obtained according to the method described by R. Seka and W. Kellermann, Chem. Ber. 75B, 1730 (1942).
• infrared spectrum (KBr), characteristic bands in cm -1 : 3550; 3250; 3200; 3140; 3125; 3060; 3020; 3000; 2400; 1705; 1645; 1555; 1505; 1460; 1385; 765 and 725!.
• the 1-(1-oxo-2-indanyl)imidazole-2-carboxamide can be prepared in the following manner: 1.35 g of ethyl 1-(1-oxo-2-indanyl)imidazole-2-carboxylate dissolved in 15 ml of methanol are introduced into 25 ml of a 2.5N ammoniacal methanol solution and the solution is preserved for 20 hours at a temperature close to 20° C. and then concentrated to dryness under reduced pressure (15 mm of Hg; 2 kPa) at 40° C.
• the product obtained is suspended in 30 ml of isopropyl ether, filtered, washed twice with a total of 20 ml of isopropyl ether and then dried under reduced pressure (15 mm of Hg; 2 kPa) at a temperature close to 20° C.
• 1.2 g of 1-(1-oxo-2-indanyl)imidazole-2-carboxamide are thus obtained in the form of a solid which melts at 183° C.
• the ethyl 1-(1-oxo-2-indanyl)imidazole-2-carboxylate can be prepared in the following manner: to a suspension of 0.4 g of 80% sodium hydride in 5 ml of anhydrous dimethylformamide kept under a nitrogen atmosphere, is added dropwise over 10 minutes at a temperature of between 20 and 25° C. a solution of 1.4 g of ethyl imidazole-2-carboxylate in 15 ml of dimethylformamide. After stirring for 15 minutes, there is added dropwise over 10 minutes a solution of 3 g of 2-bromo-1-indanone in 20 ml of dimethylformamide.
• the mixture is stirred for 1 hour then, after slowly adding 10 ml of water, poured over 400 ml of distilled water and extracted 3 times with a total of 300 ml of chloroform.
• the organic extracts are pooled, washed with 100 ml of distilled water, dried over anhydrous sodium sulphate and concentrated to dryness under reduced pressure (15 mm of Hg, 2 kPa) at 35° C.
• the product obtained (3.55 g) is chromatographed on 215 g of neutral silica gel (0.020-0.045 mm) contained in a column 4.1 cm in diameter, eluting under pressure with a dichloromethane-ethyl acetate mixture (60-40 by volume) and collecting 90-ml fractions.
• the medicinal products according to the invention consist of a compound of formula (1) or a salt of such a compound, in the pure state or in the form of a composition in which it is combined with any other pharmaceutically compatible product, which may be inert or physiologically active.
• the medicinal products according to the invention may be used orally, parenterally, rectally or topically.
• Tablets, pills, powders (gelatine capsules, cachets) or granules can be used as solid compositions for oral administration.
• the active ingredient according to the invention is mixed with one or more inert diluents such as starch, cellulose, sucrose, lactose or silica, under an argon stream.
• these compositions may also contain substances other than diluents, for example one or more lubricant such as magnesium stearate or talc, a colouring, a coating (sugar-coated tablets) or a glaze.
• compositions for oral administration can be used as liquid compositions for oral administration.
• inert diluents such as water, ethanol, glycerol, vegetable oils or paraffin oil
• compositions may contain substances other than diluents, for example wetting, sweetening, thickening, flavoring or stabilizing products.
• Sterile compositions for parenteral administration may be, preferably, aqueous or nonaqueous solutions, suspensions or emulsions.
• Water, propylene glycol, a polyethylene glycol, vegetable oils, in particular olive oil, injectable organic esters, for example ethyl oleate or other appropriate organic solvents may be used as solvent or vehicle.
• These compositions may also contain adjuvants, in particular wetting, isotonizing, emulsifying, dispersing and stabilizing agents.
• the sterilization can be performed in several ways, for example by asepticizing filtration by incorporating into the composition sterilizing agents, by irradiation or by heating. They can also be prepared in the form of sterile solid compositions which can be dissolved at the time of use in sterile water or any other injectable sterile medium.
• compositions for rectal administration are suppositories or rectal capsules which contain, in addition to the active product, excipients such as cocoa butter, semisynthetic glycerides or polyethylene glycols.
• compositions for topical administration may be for example cremes, lotions, collyria, collutories, nasal drops or sprays.
• the compounds according to the invention are particularly useful for the treatment and/or prevention of conditions which require the administration of a AMPA receptor antagonist or of an NMDA receptor antagonist.
• These compounds are especially useful for the treatment or prevention of all ischaemias and in particular cerebral ischaemia, the effects due to an anoxia, the progression of neurodegenerative diseases, of HUNTINGTON'S chorea, of ALZHEIMER's disease, of amyotrophic lateral sclerosis, of olivopontocerebellar atrophy, and of PARKINSON's disease, against epileptogenic and/or convulsive manifestations, or for the treatment of cerebral or spinal traumas, of anxiety, of depression, of schizophrenia, as analgesics, antianoretics, antiemetics, antimigraines and for the treatment of poisoning by neurotoxins or other substances which are NMDA receptor agonists, as well as neurological disorders associated with viral diseases such as AIDS, rabies, measles and tetanus.
• These compounds are also useful
• the doses depend on the desired effect, the duration of the treatment and the route of administration used; they are generally between 10 mg. and 100 mg per day orally, for an adult, with unit doses ranging from 5 mg to 50 mg of active substance.
• the doctor will determine the appropriate dosage according to the age, weight and all other factors which are specific to the subject to be treated.
• Gelatine capsules containing 50 mg doses of active product having the following composition are prepared according to the customary technique:
• Tablets containing 50 mg doses of active product having the following composition are prepared according to the customary technique:

Landscapes

• Health & Medical Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Life Sciences & Earth Sciences (AREA)
• Public Health (AREA)
• General Chemical & Material Sciences (AREA)
• Medicinal Chemistry (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Pharmacology & Pharmacy (AREA)
• Veterinary Medicine (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Heart & Thoracic Surgery (AREA)
• Cardiology (AREA)
• Biomedical Technology (AREA)
• Neurology (AREA)
• Neurosurgery (AREA)
• Hospice & Palliative Care (AREA)
• Psychiatry (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)
• Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=9434062

Family Applications (1)

Country Status (16)

Cited By (2)

Families Citing this family (12)

Citations (7)

Family Cites Families (4)

• 1992
  • 1992-10-02 FR FR9211674A patent/FR2696466B1/fr not_active Expired - Fee Related
• 1993
  • 1993-09-28 JP JP6508775A patent/JPH08501786A/ja active Pending
  • 1993-09-28 WO PCT/FR1993/000946 patent/WO1994007893A1/fr active IP Right Grant
  • 1993-09-28 US US08/406,982 patent/US5677306A/en not_active Expired - Fee Related
  • 1993-09-28 EP EP93920940A patent/EP0662971B1/de not_active Expired - Lifetime
  • 1993-09-28 PL PL93308232A patent/PL308232A1/xx unknown
  • 1993-09-28 AT AT93920940T patent/ATE166055T1/de not_active IP Right Cessation
  • 1993-09-28 HU HU9500959A patent/HUT72501A/hu unknown
  • 1993-09-28 ES ES93920940T patent/ES2116467T3/es not_active Expired - Lifetime
  • 1993-09-28 DE DE69318563T patent/DE69318563T2/de not_active Expired - Fee Related
  • 1993-09-28 CA CA002146152A patent/CA2146152A1/fr not_active Abandoned
  • 1993-09-28 AU AU48242/93A patent/AU672817B2/en not_active Ceased
  • 1993-09-28 NZ NZ256055A patent/NZ256055A/en unknown
  • 1993-09-28 DK DK93920940T patent/DK0662971T3/da active
  • 1993-09-29 ZA ZA937241A patent/ZA937241B/xx unknown
• 1995
  • 1995-03-31 FI FI951555A patent/FI951555A/fi unknown

Patent Citations (12)

Non-Patent Citations (5)

Also Published As

Similar Documents

Legal Events